Medical Device Recalls
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1 result found
510(K) Number: K201300 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Olympus Airway Mobilescope, Models MAF-DM2, MAF-GM2, & MAF-TM2. | 2 | 08/31/2023 | Olympus Corporation of the Americas |
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